TY - JOUR
T1 - Enhanced functional connectivity involving the ventromedial hypothalamus following methamphetamine exposure
AU - Zuloaga, Damian G.
AU - Iancu, Ovidiu D.
AU - Weber, Sydney
AU - Etzel, Desiree
AU - Marzulla, Tessa
AU - Stewart, Blair
AU - Allen, Charles N.
AU - Raber, Jacob
N1 - Publisher Copyright:
© 2015 Zuloaga, Iancu, Weber, Etzel, Marzulla, Stewart, Allen and Raber.
PY - 2015
Y1 - 2015
N2 - Methamphetamine (MA) consumption causes disruption of many biological rhythms including the sleep-wake cycle. This circadian effect is seen shortly following MA exposure and later in life following developmental MA exposure. MA phase shifts, entrains the circadian clock and can also alter the entraining effect of light by currently unknown mechanisms. We analyzed and compared immunoreactivity of the immediate early gene c-Fos, a marker of neuronal activity, to assess neuronal activation 2 h following MA exposure in the light and dark phases. We used network analyses of correlation patterns derived from global brain immunoreactivity patterns of c-Fos, to infer functional connectivity between brain regions. There were five distinct patterns of neuronal activation. In several brain areas, neuronal activation following exposure to MA was stronger in the light than the dark phase, highlighting the importance of considering circadian periods of increased effects of MA in defining experimental conditions and understanding the mechanisms underlying detrimental effects of MA exposure to brain function. Functional connectivity between the ventromedial hypothalamus (VMH) and other brain areas, including the paraventricular nucleus of the hypothalamus and basolateral and medial amygdala, was enhanced following MA exposure, suggesting a role for the VMH in the effects of MA on the brain.
AB - Methamphetamine (MA) consumption causes disruption of many biological rhythms including the sleep-wake cycle. This circadian effect is seen shortly following MA exposure and later in life following developmental MA exposure. MA phase shifts, entrains the circadian clock and can also alter the entraining effect of light by currently unknown mechanisms. We analyzed and compared immunoreactivity of the immediate early gene c-Fos, a marker of neuronal activity, to assess neuronal activation 2 h following MA exposure in the light and dark phases. We used network analyses of correlation patterns derived from global brain immunoreactivity patterns of c-Fos, to infer functional connectivity between brain regions. There were five distinct patterns of neuronal activation. In several brain areas, neuronal activation following exposure to MA was stronger in the light than the dark phase, highlighting the importance of considering circadian periods of increased effects of MA in defining experimental conditions and understanding the mechanisms underlying detrimental effects of MA exposure to brain function. Functional connectivity between the ventromedial hypothalamus (VMH) and other brain areas, including the paraventricular nucleus of the hypothalamus and basolateral and medial amygdala, was enhanced following MA exposure, suggesting a role for the VMH in the effects of MA on the brain.
KW - Activation
KW - Dark phase
KW - Functional connectivity
KW - Light phase
KW - Methamphetamine
UR - http://www.scopus.com/inward/record.url?scp=84949657809&partnerID=8YFLogxK
U2 - 10.3389/fnins.2015.00326
DO - 10.3389/fnins.2015.00326
M3 - Article
AN - SCOPUS:84949657809
SN - 1662-4548
VL - 9
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
IS - SEP
M1 - 326
ER -